1,090 results on '"Santoro, Lucio"'
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2. Daytime sleepiness and sleep quality in Charcot–Marie–Tooth disease
3. Autonomic dysfunction is associated with disease progression and survival in amyotrophic lateral sclerosis: a prospective longitudinal cohort study
4. Correction to: Daytime sleepiness and sleep quality in Charcot–Marie–Tooth disease
5. Anxiety and depression in Charcot-Marie-Tooth disease: data from the Italian CMT national registry
6. A compound score to screen patients with hereditary transthyretin amyloidosis
7. Electromyography
8. Cardiovascular autonomic failure correlates with cutaneous autonomic devervation in PD and MSA
9. Prolonged distal motor latency of median nerve does not improve diagnostic accuracy for CIDP
10. Muscle Pain, Weakness and/or Sensory Disorders
11. The neurophysiological lesson from the Italian CIDP database
12. The impact of symptoms on daily life as perceived by patients with Charcot-Marie-Tooth type 1A disease
13. Skin innervation across amyotrophic lateral sclerosis clinical stages: new prognostic biomarkers.
14. Use, tolerability, benefits and side effects of orthotic devices in Charcot-Marie-Tooth disease.
15. Postganglionic Sudomotor Assessment in Early Stage of Multiple System Atrophy and Parkinson Disease: A Morpho-functional Study
16. The electrophysiology of axonal neuropathies: More than just evidence of axonal loss
17. Alteration of the late endocytic pathway in Charcot–Marie–Tooth type 2B disease
18. A 5-year clinical follow-up study from the Italian National Registry for FSHD
19. Skin innervation across amyotrophic lateral sclerosis clinical stages: new prognostic biomarkers
20. Electrodiagnostic accuracy in polyneuropathies: supervised learning algorithms as a tool for practitioners
21. In vivo evidence of cortical amyloid deposition in the adult form of Niemann Pick type C
22. Different cortical excitability profiles in hereditary brain iron and copper accumulation
23. Muscle Pain, Weakness and/or Sensory Disorders
24. Brainstem involvement and respiratory failure in COVID-19
25. Increased peptidergic fibers as a potential cutaneous marker of pain in diabetic small fiber neuropathy
26. Six-minute walk test is reliable and sensitive in detecting response to therapy in CIDP
27. microRNAs as biomarkers in Pompe disease
28. Large genotype–phenotype study in carriers of D4Z4 borderline alleles provides guidance for facioscapulohumeral muscular dystrophy diagnosis
29. Pregnancy in Charcot-Marie-Tooth disease: Data from the Italian CMT national registry
30. Electromyography
31. Long-term therapy with miglustat and cognitive decline in the adult form of Niemann-Pick disease type C: a case report
32. Subclinical neurological involvement does not develop if Wilson's disease is treated early
33. The Effect of Cerebellar Degeneration on Human Sensori-motor Plasticity
34. Next generation sequencing on patients with LGMD and nonspecific myopathies: Findings associated with ANO5 mutations
35. Phosphorylated α-Synuclein Deposits in Cutaneous Nerves of Early Parkinsonism
36. Small fiber pathology parallels disease progression in Parkinson disease: a longitudinal study
37. Early predictive factors of disability in CIDP
38. The occurrence of lateral shift in cervical dystonia
39. Selected items from the Charcot-Marie-Tooth (CMT) Neuropathy Score and secondary clinical outcome measures serve as sensitive clinical markers of disease severity in CMT1A patients
40. Targeted transcript analysis in muscles from patients with genetically diverse congenital myopathies
41. Cardiovascular autonomic failure correlates with cutaneous autonomic denervation and patient symptoms in alpha-synucleinopathies
42. Clinical and Neuropsychological Long-Term Outcomes After Late Recovery of Responsiveness: A Case Series
43. Muscle pain syndromes and fibromyalgia: the role of muscle biopsy
44. Autosomal-dominant transthyretin (TTR)-related amyloidosis is not a frequent CMT2 neuropathy “in disguise”
45. Influence of comorbidities on the phenotype of patients affected by Charcot–Marie–Tooth neuropathy type 1A
46. Sporadic chronic progressive external ophthalmoplegia with single large mitochondrial DNA deletion and neurogenic findings
47. A novel clinical tool to classify facioscapulohumeral muscular dystrophy phenotypes
48. Short-latency afferent inhibition in patients with Parkinson’s disease and freezing of gait
49. Centronuclear myopathy related to dynamin 2 mutations: Clinical, morphological, muscle imaging and genetic features of an Italian cohort
50. Electrodiagnosis of Guillain-Barre syndrome in the International GBS Outcome Study: Differences in methods and reference values.
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